PEDICRAFT BED, MODEL B2944— 510(k) K821773

Substantially Equivalent

Pedicraft, Inc.

FDA 510(k) clearance K821773 for PEDICRAFT BED, MODEL B2944, Substantially Equivalent on 1982-06-23. Applicant: Pedicraft, Inc.. Device class: 2.

Clearance details

Applicant: Pedicraft, Inc.
Product code: Code FMS
Device class: Class 2
Regulation: 21 CFR 880.5140
Advisory panel: General Hospital
Date received: 1982-06-16
Decision date: 1982-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FMS

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K960012 — STRYKER ADEL BASSINET1996-03-25
K951024 — NATURE'S CRADLE1995-06-05

More clearances from Pedicraft, Inc.

K925817 — HEAD & FOOT END DROP PEDI-CRIB1993-04-20
K925949 — PEDICRAGT BASSINET1993-04-20
K905629 — PEDICRAFT INFANT REFLUX WEDGE1991-03-13
K905630 — INFANT REFLUX SLING1991-03-13

Data sourced from openFDA. This site is unofficial and independent of the FDA.